Scientist Jobs at ProPharma | Apply Now for Pharmacovigilance Safety
Are you looking for an exciting opportunity to contribute to global healthcare safety? ProPharma, a trusted partner to biotech, medical device, and pharmaceutical organizations worldwide, is hiring a Pharmacovigilance Safety Scientist in India. This role offers you the chance to play a pivotal part in advancing patient safety through pharmacovigilance, risk management, and regulatory compliance, while working with industry leaders who are shaping the future of drug safety.
About the Company
ProPharma is the world’s largest Research Consulting Organization (RCO), delivering end-to-end support across the product lifecycle for life sciences companies. Through its unique advise-build-operate model, ProPharma helps organizations de-risk, accelerate, and optimize scientific and regulatory programs. With a focus on pharmacovigilance, clinical development, and regulatory science, ProPharma empowers innovation that improves patient outcomes across the globe.
Job Details
- Job Post: Pharmacovigilance Safety Scientist
- ID: JR 7763
Educational & Experience Requirements
- Bachelor’s or Master’s degree in Pharmacy, Nursing, Life Sciences, or related fields.
- Minimum 2 years’ experience in pharmacovigilance, with expertise in medical writing, literature search, or signal detection.
- Proven experience in authoring aggregate reports, literature screening, and pharmacovigilance documentation.
- Proficiency in IT systems and MS Office Suite (Word, Excel, PowerPoint).
About the Role
The Pharmacovigilance (PV) Safety Scientist will support the Benefit Risk group by ensuring day-to-day operational activities are managed efficiently. This role requires professionalism, scientific accuracy, and collaboration with senior PV Scientists and management to maintain high-quality safety standards.
Key Responsibilities
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Author aggregate reports including PSURs, PBRERs, PADERs, Annual Reports, ACO, and DSUR for submission to health authorities.
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Prepare Risk Management Plans (RMPs) and Signal Management Reports.
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Perform literature searches and ensure data validity for aggregate reports.
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Extract, validate, and reconcile safety-related data, including RSI, sales, RMP, and signal information.
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Generate Line Listings (LL) from safety databases.
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Provide reliable support for high-priority ad-hoc pharmacovigilance activities.
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Ensure deliverables comply with regulatory requirements and are submitted on time.
Required Skills
Strong analytical skills, attention to detail, and the ability to work within a professional team environment. A clear understanding of ICH-GCP, FDA, EMA, and global pharmacovigilance regulations is essential. The candidate must demonstrate excellent medical writing skills, data interpretation, and the ability to produce concise and accurate safety documentation.
Why Join ProPharma?
By joining ProPharma, you become part of a collaborative, diverse, and inclusive workplace that values authenticity, growth, and innovation. This role provides exposure to global drug safety operations and offers the opportunity to make a meaningful impact on patient safety worldwide.
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